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DOID:397 - restrictive cardiomyopathy
Disease Ontology Definition:An intrinsic cardiomyopathy characterized by impaired ventricular filling, with normal or decreased diastolic volume of either or both ventricles typically resulting from increased stiffness of the myocardium.
Synonyms: Cardiomyopathy, constrictive, Familial restrictive cardiomyopathy, primary restrictive cardiomyopathy, primary restrictive cardiomyopathy (disorder), Restrictive cardiomyopathy, Restrictive cardiomyopathy (disorder)
Xenbase Genes
:
tnnt2,
tnni3,
mypn
| MONDO:0005201 - restrictive cardiomyopathy |
| MIM:115210 - CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1; RCM1 |
| MIM:612422 - CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3; RCM3 |
| MIM:615248 - CARDIOMYOPATHY, DILATED, 1KK; CMD1KK |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
intrinsic cardiomyopathy (is_a)